Visitor Monitoring Drug Details: GLYBURIDE (MICRONIZED)
 
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Drug Details

Drug Name: GLYBURIDE (MICRONIZED)
FDA Application No: (NDA) 020055
Active Ingredient(s): GLYBURIDE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: April 17, 1992
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
GLYBURIDE (MICRONIZED) GLYBURIDE1.5MGTABLET; ORAL Discontinued No None
GLYBURIDE (MICRONIZED) GLYBURIDE3MGTABLET; ORAL Discontinued No None
GLYBURIDE (MICRONIZED) GLYBURIDE6MGTABLET; ORAL Discontinued No None


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